A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040665



Internal ID18783196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30515727..30687726hg38UCSC Ensembl
Innerchr15:30807930..30979929hg19UCSC Ensembl
Innerchr15:28595222..28767221hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38172000
hg19172000
hg18172000
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2527n100
Supporting Variantsnssv3547606
Samples
Known GenesARHGAP11B, GOLGA8H, LOC100288637, ULK4P1, ULK4P2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1040665
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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